A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3511096



Internal ID18809377
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:58418031..58469218hg38UCSC Ensembl
Innerchr10:60177791..60228978hg19UCSC Ensembl
Innerchr10:59847797..59898984hg18UCSC Ensembl
Cytoband10q21.1
Allele length
AssemblyAllele length
hg3851188
hg1951188
hg1851188
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1041314
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3511096
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer